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dc.contributor.authorAravantinos, Gerasimosen
dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorKosmidis, Paraskevas A.en
dc.contributor.authorDimopoulos, M. A.en
dc.contributor.authorStathopoulos, G. P.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorBafaloukos, Dimitriosen
dc.contributor.authorPapadimitriou, C.en
dc.contributor.authorKarpathios, S.en
dc.contributor.authorGeorgoulias, V.en
dc.contributor.authorPapakostas, P.en
dc.contributor.authorKalofonos, H. P.en
dc.contributor.authorGrimani, E.en
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.creatorAravantinos, Gerasimosen
dc.creatorFountzilas, Georgeen
dc.creatorKosmidis, Paraskevas A.en
dc.creatorDimopoulos, M. A.en
dc.creatorStathopoulos, G. P.en
dc.creatorPavlidis, Nicholasen
dc.creatorBafaloukos, Dimitriosen
dc.creatorPapadimitriou, C.en
dc.creatorKarpathios, S.en
dc.creatorGeorgoulias, V.en
dc.creatorPapakostas, P.en
dc.creatorKalofonos, H. P.en
dc.creatorGrimani, E.en
dc.creatorSkarlos, Dimosthenis V.en
dc.date.accessioned2018-06-22T09:52:26Z
dc.date.available2018-06-22T09:52:26Z
dc.date.issued2005
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41352
dc.description.abstractBackground: We compared the combination plus Carboplatin plus paclitaxel, which is considered the treatment of choice for initial chemotherapy of advanced ovarian cancer (AOC) with a regimen combining alternating carboplatin and cisplatin plus paclitaxel. The two platinum derivatives have been previously combined as they are not totally cross-resistant and as they share no overlapping toxicities. Patients and methods: Patients with AOC, after the initial cytoreductive surgery were randomized to either 6 courses of paclitaxel at 175 mg/m2 as 3h infusion plus Carboplatin at 7 AUC (Arm A) or Paclitaxel at the same dose plus Carboplatin again at 7 AUC for cycles 1,3,5, while for cycles 2,4,6 Cisplatin at 75 mg/m2 substituted for Carboplatin (Arm B). Results: 247 patients are analyzed. Significant differences were not found, both in terms of PFS (38 vs 39 months, p=0.95) and overall survival (40.6 vs 38.6 months, p=0.79). There was not also difference in 5-year survival rate (35% vs 39%) or 5-year PFS rate (23% vs 28%). Age >60, PS 2, stage IV disease and presence of residual disease were adversely related to the overall survival. Conclusion: Both regimens are well tolerated and effective. Alternating cisplatin with carboplatin does not improve the results compared with the standard combination. © 2005 European Society fr Medical Oncology.en
dc.language.isoengen
dc.sourceAnnals of Oncologyen
dc.subjectArticleen
dc.subjectAntineoplastic agenten
dc.subjectCisplatinen
dc.subjectHumanen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectCancer patienten
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectAdvanced canceren
dc.subjectCarboplatinen
dc.subjectChemotherapyen
dc.subjectOvarian canceren
dc.subjectOvarian neoplasmsen
dc.subjectOvary canceren
dc.subjectPaclitaxelen
dc.subjectPriority journalen
dc.subjectAnemiaen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectArthralgiaen
dc.subjectClinical trialen
dc.subjectControlled clinical trialen
dc.subjectDisease-free survivalen
dc.subjectDrug efficacyen
dc.subjectFatigueen
dc.subjectFebrile neutropeniaen
dc.subjectInfectionen
dc.subjectLeukopeniaen
dc.subjectMucosa inflammationen
dc.subjectMulticenter studyen
dc.subjectMyalgiaen
dc.subjectNausea and vomitingen
dc.subjectNeurotoxicityen
dc.subjectNeutropeniaen
dc.subjectOndansetronen
dc.subjectProspective studiesen
dc.subjectRecombinant granulocyte colony stimulating factoren
dc.subjectThrombocytopeniaen
dc.subjectNephrotoxicityen
dc.subjectSurvival analysisen
dc.subjectAlternating cisplatin with carboplatinen
dc.subjectArea under the curveen
dc.subjectCancer stagingen
dc.subjectCardiotoxicityen
dc.subjectCimetidineen
dc.subjectCytoreductive surgeryen
dc.subjectDexamethasoneen
dc.subjectDimetindeneen
dc.subjectDisease free survivalen
dc.subjectDrug administrationen
dc.subjectDrug administration scheduleen
dc.subjectDrug dose regimenen
dc.subjectDrug fatalityen
dc.subjectDrug hypersensitivityen
dc.subjectDrug tolerabilityen
dc.subjectFeveren
dc.subjectGastrointestinal toxicityen
dc.subjectGranulocyte colony stimulating factoren
dc.subjectHeart ventricle arrhythmiaen
dc.subjectInitial treatmenten
dc.subjectLiver toxicityen
dc.subjectMinimal residual diseaseen
dc.subjectOvary tumoren
dc.subjectPainen
dc.subjectPatient complianceen
dc.subjectPhase 3 clinical trialen
dc.subjectPneumoniaen
dc.subjectPromethazineen
dc.subjectProspective studyen
dc.subjectRandomized controlled trialen
dc.subjectStandardizationen
dc.subjectStatistical significanceen
dc.subjectSurvivalen
dc.subjectSurvival rateen
dc.subjectTreatment outcomeen
dc.titlePaclitaxel plus carboplatin versus paclitaxel plus alternating carboplatin and cisplatin for initial treatment of advanced ovarian cancer: Long-term efficacy results: A Hellenic Cooperative Oncology Group (HeCOG) studyen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1093/annonc/mdi223
dc.description.volume16
dc.description.issue7
dc.description.startingpage1116
dc.description.endingpage1122
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidPavlidis, Nicholas [0000-0002-2195-9961]
dc.contributor.orcidAravantinos, Gerasimos [0000-0002-2106-1713]
dc.contributor.orcidKalofonos, H. P. [0000-0002-3286-778X]
dc.gnosis.orcid0000-0002-2195-9961
dc.gnosis.orcid0000-0002-2106-1713
dc.gnosis.orcid0000-0002-3286-778X


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